916497-81-9

Basic information

• Product Name: p-octyloxyphenyl 2-deoxy-2-phthalimido-3,4,6-tri-O-acetyl-1-thio-β-D-glucopyranoside
• Synonyms: p-octyloxyphenyl 2-deoxy-2-phthalimido-3,4,6-tri-O-acetyl-1-thio-β-D-glucopyranoside
• CAS NO: 916497-81-9
• Molecular Weight: 655.766
• Mol File: 916497-81-9.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: p-octyloxyphenyl 2-deoxy-2-phthalimido-3,4,6-tri-O-acetyl-1-thio-β-D-glucopyranoside(CAS DataBase Reference)
• NIST Chemistry Reference: p-octyloxyphenyl 2-deoxy-2-phthalimido-3,4,6-tri-O-acetyl-1-thio-β-D-glucopyranoside(916497-81-9)
• EPA Substance Registry System: p-octyloxyphenyl 2-deoxy-2-phthalimido-3,4,6-tri-O-acetyl-1-thio-β-D-glucopyranoside(916497-81-9)

Safety Data

• Hazardous Substances Data: 916497-81-9(Hazardous Substances Data)

Upstream product

• 72858-55-0 3,4,6-tri-O-acetyl-2-deoxy-2-phthalimido-D-glucopyranose 
• 102231-96-9 p-octyloxybenzenethiol 
• 10022-13-6 1,3,4,6-tetra-O-acetyl-2-deoxy-2-phthalimido-β-D-glucopyranose 
• 21095-40-9 4-(octyloxy)benzene-1-sulfonyl chloride 

Downstream Products

• 1242660-03-2 3,4,6-tri-O-acetyl-2-N-phthaloyl-β(1-2)-D-glucosaminyl-3-O-benzyl-(4,6)-benzylidene-β-D-mannopyranosyl p-octyloxyphenyl sulfoxide 
• 1242660-00-9 3,4,6-tri-O-acetyl-2-N-phthaloyl-β(1-6)-D-glucosaminyl-2,3,4-tri-O-benzyl-β-D-glucopyranosyl p-octyloxyphenyl sulfoxide 
• 1010692-62-2 C₇₂H₈₁NO₂₀Si 

Relevant articles and documents

Glycosylation reaction of thioglycosides by using hypervalent iodine(III) reagent as an excellent promoter

Thioglycosides are available donors in glycosylation due to the stability of the anomeric C-S bond under general reaction conditions of protection and deprotection, and offer orthogonality in their activation. We report now that the hypervalent iodine eff

Odorless benzenethiols in synthesis of thioglycosides and its application for glycosylation reactions

p-Octyloxybenzenethiol (2) was synthesized as a new odorless benzenethiol. Moreover, preparation of thioglycosides using 2 and their application for glycosylation reactions were attempted. As a result, it was found that the thioglycosides were as excellen